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SIGMA 2024-46-020Recalls & reported problems

Depuy (Ireland) · SIGMA HP PARTIAL KNEE TIBIAL PEG DRILL · Class 1

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295083177), received between May 19, 2023 and May 19, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Cut” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Failure to Cut1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 19, 2023Failure to Cut; Failure to Cut

    IT WAS REPORTED THAT THE TIBIAL PEG DRILL WAS BECOMING BLUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16962663 ↗

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Sources and updates

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